Department of Materials Science and Engineering, National University of Singapore, Singapore, 117573, Singapore.
Institute of Chemical and Engineering Sciences, Agency for Science, Technology and Research, Singapore, 627833, Singapore.
Adv Mater. 2022 Dec;34(50):e2107956. doi: 10.1002/adma.202107956. Epub 2022 Nov 18.
The electron-transfer process during the oxygen evolution reaction (OER) often either proceeds solely via a metal redox chemistry (adsorbate evolution mechanism (AEM), with metal bands around the Fermi level) or an oxygen redox chemistry (lattice oxygen oxidation mechanism (LOM), with oxygen bands around the Fermi level). Unlike the AEM, the LOM involves oxygen redox chemistry instead of metal redox, which leads to the formation of a direct oxygen-oxygen (OO) bond. As a result, such a process is able to bypass the rate-determining step, that is, OO bonding, in AEM, which highlights the critical advantage of LOM as compared to the conventional AEM. Thus, it has been well reported that LOM-based catalysts are able to demonstrate higher OER activities as compared to AEM-based catalysts. Here, a comprehensive understanding of the oxygen redox in LOM and all documented and possible characterization techniques that can be used to identify the oxygen redox are reviewed. This review will interpret the origins of oxygen redox in the reported LOM-based electrocatalysts and the underlying science of LOM-induced surface reconstruction in transition metal oxides. Finally, perspectives on the future development of LOM electrocatalysts are also provided.
在氧气析出反应(OER)过程中,电子转移过程通常仅通过金属氧化还原化学(吸附物演化机制(AEM),费米能级周围的金属能带)或氧氧化还原化学(晶格氧氧化机制(LOM),费米能级周围的氧能带)进行。与 AEM 不同,LOM 涉及氧氧化还原化学而不是金属氧化还原,这导致直接氧-氧(OO)键的形成。因此,这样的过程能够绕过 AEM 中的速率决定步骤,即 OO 键合,这凸显了 LOM 相对于传统 AEM 的关键优势。因此,已有大量报道表明,基于 LOM 的催化剂比基于 AEM 的催化剂具有更高的 OER 活性。在这里,全面了解 LOM 中的氧氧化还原以及所有有记录和可能的可用于识别氧氧化还原的特征技术进行了综述。本综述将解释在报道的基于 LOM 的电催化剂中氧氧化还原的起源以及 LOM 诱导的过渡金属氧化物表面重构的基础科学。最后,还对 LOM 电催化剂的未来发展提供了展望。